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2-Amino-3-methylbutan-1-ol

Names

[ CAS No. ]:
16369-05-4

[ Name ]:
2-Amino-3-methylbutan-1-ol

[Synonym ]:
2-amino-3-methylbutan-1-ol
1-Butanol, 2-amino-3-methyl-
DL-2-Amino-3-methyl-1-butanol
QVYZY1&1
EINECS 240-425-0
valinol
1-Butanol, 2-amino-3-methyl-,
MFCD00004730
2-Amino-3-methyl-1-butanol

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
186.8±13.0 °C at 760 mmHg

[ Melting Point ]:
31-32℃

[ Molecular Formula ]:
C5H13NO

[ Molecular Weight ]:
103.163

[ Flash Point ]:
91.1±0.0 °C

[ Exact Mass ]:
103.099716

[ PSA ]:
46.25000

[ LogP ]:
-0.08

[ Vapour Pressure ]:
0.2±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.447

[ Storage condition ]:
Refrigerator (+4°C)

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
UN 2735

[ WGK Germany ]:
3

[ HS Code ]:
2922199090

Precursor & DownStream

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.

Chemistry 9(22) , 5567-80, (2003)

Four new chiral bis(amino alcohol)oxalamides (1-4: amino alcohol=leucinol, valinol, phenylglycinol, and phenylalaninol, respectively) have been prepared as low-molecular-weight organic gelators. Their...

Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.

J. Org. Chem. 74(16) , 5822-38, (2009)

trans-N-(Arenesulfonyl)-2-tributylstannyloxazolidines derived from (R)-phenylglycinol were diastereoselectively ring-opened by soft organometallic reagents in the presence of BF(3).OEt(2). Both higher...

General synthesis route to benanomicin-pradimicin antibiotics.

Chemistry 13(35) , 9791-823, (2007)

A general approach to the regio- and stereoselective total synthesis of the benanomicin-pradimicin antibiotics (BpAs) is described. Construction of the aglycon has been achieved by 1) the diastereosel...


More Articles


Related Compounds

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